9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
TURBOX
FDA 510(k)
FDA Class 1
·Immunology
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·August 16, 2012
EARPOPPER, MODEL EP-2000, EP-2100, EP-3000
FDA 510(k)
FDA Unclassified
·Unknown
COAT-A-COUNT TESTOSTERONE RIA KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MALLINKRODT
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·August 17, 2010
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FPA·June 13, 2014
M2A-MAGNUM 42-50MM TPR INSRT-3
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·December 14, 2012
IAB: 8FR - 40 CC
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·September 20, 2010
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024